Overview

This trial is active, not recruiting.

Conditions arterial access, peripheral access, central venous catheter
Treatment bedside point-of-care device
Sponsor Joseph D. Tobias
Start date September 2015
End date November 2016
Trial size 50 participants
Trial identifier NCT02888431, IRB15-00793

Summary

The purpose of this study is to determine the correlation between pH, base deficit, and lactate values when comparing venous and arterial blood samples in the pediatric population.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective
Arm
0.5 mL blood sample from arterial line which is clinically indicated
bedside point-of-care device
A bedside point-of-care device is routinely used in the operating room to measure lactate, base deficit, and pH.
0.5 mL blood sample drawn simultaneously with arterial sample from clinically indicated peripheral line
bedside point-of-care device
A bedside point-of-care device is routinely used in the operating room to measure lactate, base deficit, and pH.

Primary Outcomes

Measure
lactate blood value
time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)
base deficit blood value
time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)
pH blood value
time frame: During surgery- approximately 15-20 minutes after induction in the operating room (OR)

Eligibility Criteria

Male or female participants of any age.

Inclusion Criteria: - Patients requiring arterial access and peripheral access. Additionally, patients with a central venous catheter would be included. Exclusion Criteria: - Patients who not require arterial access.

Additional Information

Principal investigator Joseph Tobias
Trial information was received from ClinicalTrials.gov and was last updated in August 2016.
Information provided to ClinicalTrials.gov by Nationwide Children's Hospital.